drug review process

The drug review process involves several steps to ensure a medication's safety, effectiveness, and quality before it reaches patients. After a company develops a drug, they submit detailed data to regulatory agencies like the FDA. Experts then evaluate this data through rigorous review, examining clinical trial results, manufacturing practices, and potential risks. They may ask for additional information or studies. Once approved, the drug can be marketed, but ongoing monitoring continues to identify any rare side effects or issues. This process aims to protect public health by ensuring only safe and effective medications are available.